Variant: rs1016343 

    present in Gene: PCAT2;PCAT1;PRNCR1;CASC19
    present in Chromosome: 8
    Position on Chromosome: 127081052
    Alleles of this Variant: C/T

rs1016343 in PCAT2;PCAT1;PRNCR1;CASC19 gene and Malignant neoplasm of prostate PMID 23555315 2013 Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.

PMID 18264097 2008 Multiple newly identified loci associated with prostate cancer susceptibility.

PMID 22923026 2012 Evaluating genetic risk for prostate cancer among Japanese and Latinos.

PMID 21743057 2011 Genome-wide association study identifies new prostate cancer susceptibility loci.

rs1016343 in PCAT2;PCAT1;PRNCR1;CASC19 gene and Nasopharyngeal carcinoma PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.

rs1016343 in PCAT2;PCAT1;PRNCR1;CASC19 gene and Prostate carcinoma PMID 26034056 2015 A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.

PMID 18264097 2008 Multiple newly identified loci associated with prostate cancer susceptibility.

PMID 21743057 2011 Genome-wide association study identifies new prostate cancer susceptibility loci.

PMID 17401366 2007 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.